4-Bromo-2-fluoro-6-methylbenzonitrile

≥95%

Reagent Code: #79505
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CAS Number 1427438-75-2

science Other reagents with same CAS 1427438-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.03 g/mol
Formula C₈H₅BrFN
badge Registry Numbers
MDL Number MFCD21337355
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily used in the field of organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, fluoro, and methyl groups attached to a benzonitrile core, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create compounds with potential biological activity. Additionally, its presence in research and development is notable in the creation of novel compounds for drug discovery, where its unique substitution pattern can influence the pharmacokinetics and efficacy of the final product.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,723.00
inventory 100mg
10-20 days ฿1,575.00
inventory 250mg
10-20 days ฿2,637.00
inventory 5g
10-20 days ฿21,618.00

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4-Bromo-2-fluoro-6-methylbenzonitrile
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This compound is primarily used in the field of organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, fluoro, and methyl groups attached to a benzonitrile core, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create compounds with potential biological activity. Additionally, its presence in rese

This compound is primarily used in the field of organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, fluoro, and methyl groups attached to a benzonitrile core, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create compounds with potential biological activity. Additionally, its presence in research and development is notable in the creation of novel compounds for drug discovery, where its unique substitution pattern can influence the pharmacokinetics and efficacy of the final product.

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